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Reprocessed Stanley Bed Alarm

Stryker Reprocessed Stanley Bed Alarm User manual

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Reprocessed by
Instructions for Use
Reprocessed Stanley® Bed Alarm Sensormat® Pad
Reprocessed Device for Single Patient Use
Caution: Federal (U.S.A.) law restricts this device to sale by or on the order of a physician.
• NON-STERILE
• Exposed to Ethylene Oxide (EO) gas
Explanation of Symbols
Date of Reprocessing
Do Not Reuse
See Instructions For Use
Stryker Sustainability Solutions, Inc. © 2020
1810 W Drake Dr.
Tempe AZ, 85283
sustainability.stryker.com
888.888.3433
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Reprocessed Stanley® Bed Alarm Sensormat® Pad Description
The Reprocessed STANLEY® Bed Alarm Sensormat® Pads are sensor pads designed for use with STANLEY® Fall Alarms to
detect when a patient has taken weight off the sensor to help notify nurses and caregivers that the patient has gotten up from a
sitting or resting position.
Indications for Use
The Stryker Sustainability Solutions Reprocessed STANLEY® Bed Alarm Sensormat® Pads are designed to sense body-weight
distributed over an area to detect when the patient lifts off the bed.
Warnings and Precautions
• Read all instructions carefully prior to use. Failure to do so could result in injury of a person in your care.
• Always test the system before each use.
• Model 74010FA Sensormat® pads are not recommended for persons weighing less than 80 lbs.
• Model 74030 and 92010 Sensormat® pads are not recommended for persons weighing less than 70 lbs.
• Sensormat® pads can be defeated by a cognitively aware person, a person with only a few moments of lucidity or an
uncooperative person. Properly assess each individual before a Sensormat® pad is used.
• The device should not be considered a substitute for routine staff visual monitoring consistent with your facility protocols
or other regulations.
• Keep the Sensormat® pad flat at all times. Do not bend, fold, roll, submerge in liquid, or tamper with Sensormat® pad. If the
Sensormat® pad is folded, it may not function properly.
• Sterilization by heat, gas or radiation voids all warranties.
• For model 74030, use only with STANLEY® Healthcare M200, Bed-Check®, UMP® or Micro-Tech® brand fall monitors.
• For model 74010FA, use only with STANLEY® Healthcare M200 or Bed-Check® brand fall monitors.
• For model 92010, use only with Bed-Check®, UMP® or Micro-Tech® brand fall monitors.
• For single patient use only.
• Only incontinence pads and mattress covers should be placed between pad and patient.
• For model 74010FA, using enclosed elastic bands and clips, secure the pad to bedsprings, bed frame, or mattress piping.
• Route the cable to the monitor so that it does not cross the pad surface, is not a trip hazard, and cannot be damaged by bed
or gurney mechanisms.
• Follow the Monitor User Guide procedures to connect the pad’s cable, and to test system functions.
• Before each use and then daily thereafter, test system functions and check the pad’s expiration date. If any test fails or the
pad has expired, discard the pad and DO NOT place it into service.
• Sensormat® pads may not be effective with air type bed mattresses or air type chair cushion pads; test before using.
• Operators of this equipment must be familiar with the functions and usage described in the Monitor User Guide, and must
be properly trained in the resident care policies and procedures of the facility.
Directions for Use
1. Read all Sensormat® pad and alarm instructions prior to use.
2. Check that Sensormat® pad, cord, and plug are clean and undamaged. Discard entire sensor if there is any damage.
3. When putting sensor pad into use, record the first use date and calculate expiration date from initial use.
4. Place the Sensormat® pad across the width of the bed, on top of the mattress with the labeled side up.
5. The preferred pad location is directly under the patient/resident’s buttocks 8 to 13 cm (three to five inches) below the
bend in the mattress when the head of the bed is elevated (refer to Figure 1).
a. Effective operation of the Sensormat® pad in the alternative location, behind the patient/resident’s back, is
dependent upon their weight and the articulation angle of the bed (refer to Figure 1).
6. For model 74010FA, secure the Sensormat® pad to the bedsprings, bed frame, or mattress piping with attached clips.
7. Plug the Sensormat® pad into the fall monitor and test before using (refer to Directions for Testing Sensormat® Pad).
Directions for Testing Sensormat® Pad
1. Plug the Sensormat® pad into the alarm monitor.
2. Apply FULL and FIRM palm pressure with your hand to the Sensormat® pad, and then remove pressure to make sure local
audible alarm is functioning properly.
3. Repeat this pressure/release test in several different areas along the entire length of the sensor pad to ensure entire
sensor pad functions properly.
4. If nurse call is used, make sure connections are properly made and functioning correctly.
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Storage and Handling
• This device is designed for use in normal indoor environments.
• This device may be stored in ambient warehouse temperatures at normal humidity levels. Avoid excess moisture or high
humidity that may damage product materials.
Compatibility
• For model 74030, use only with STANLEY® Healthcare M200, Bed-Check®, UMP® or Micro-Tech® brand fall monitors.
• For model 74010FA, use only with STANLEY® Healthcare M200 or Bed-Check® brand fall monitors.
• For model 92010, use only with Bed-Check®, UMP® or Micro-Tech® brand fall monitors.
Figure 1 – STANLEY® Bed Alarm Sensormat® Pad Positioning
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Warranty
74030 - This product is warrantied for up to 14 days from recorded “in-use date,” in accordance with Stryker’s standard
limited warranty.
74010FA - This product is warrantied for up to 30 days from recorded “in-use date,” in accordance with Stryker’s standard
limited warranty.
92010 – This product is warrantied for up to 45 days from recorded “in-use date,” in accordance with Stryker’s standard
limited warranty.
Reprocessed Products
Unless agreed otherwise in writing, Stryker warrants all reprocessed products, subject to the exceptions provided herein, to be
free from defects in reprocessing and to substantially conform to the product specifications contained in the documentatio n
provided by Stryker with the products for one use in accordance with the instructions for use of such product.
STRYKER SHALL NOT BE LAIBLE FOR ANY DAMAGES TO THE EXTENT CAUSED BY ANY DEFECT IN
MATERIAL, WORKMANSHIP OR DESIGN BY THE ORIGINAL MANUFACTURER OF THE PRODUCT OR ANY ACT
OR OMISSION OF THE ORIGINAL MANUFACTURER OF THE PRODUCT.
Products for which Stryker is the Original Manufacturer
Stryker warrants all products for which it is the original manufacturer, subject to the exceptions provided herein, to be free
from defects in design, materials and workmanship and to substantially conform to the product specifications contained in the
documentation provided by Stryker with the products for a period of one year from the date of purchase.
General Warranty Terms Applicable to All Products
TO THE FULLEST EXTENT PERMITTED BY LAW, THE EXPRESS WARRANTY SET FORTH HEREIN IS THE ONLY
WARRANTY APPLICABLE TO THE PRODUCTS AND IS EXPRESSLY IN LIEU OF ANY OTHER WARRANTY BY
STRYKER, EXPRESSED OR IMPLIED, INCLUDING, BUT NOT LIMITED TO, ANY IMPLIED WARRANTY OR
MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. IN NO EVENT WILL STRYKE R’S LIABILITY
ARISING IN CONNECTION WITH THE SALE OF THE PRODUCT (WHETHER UNDER THE THEORIES OF BREACH
OF CONTRACT, TORT, MISREPRESENTATION, FRAUD, WARRANTY, NEGLIGENCE, STRICT LIABILITY OR ANY
OTHER THEORY OF LAW) EXCEED THE PURCHASE PRICE, CURRENT MARKET VALUE OR RESIDUAL VALUE
OF THE PRODUCTS, WHICHEVER IS LESS. STRYKER SHALL NOT BE LIABLE FOR INDIRECT, SPECIAL,
INCIDENTAL, PUNITIVE OR CONSEQUENTIAL DAMAGES RESULTING FROM ANY BREACH OF WARRANTY OR
UNDER ANY OTHER LEGAL THEORY.
This warranty shall apply only to the original end-user purchaser of products directly from Stryker or a Stryker authorized
distributor. This warranty may not be transferred or assigned without the express written consent of Stryker.
This warranty does not apply to: (1) products that have been misused, neglected, modified, altered, adjusted, tampered with,
improperly installed or refurbished; (2) products that have been repaired by any person other than Stryker personnel
without the prior written consent of Stryker; (3) products that have been subjected to unusual stress or have not been
maintained in accordance with the instructions in the user manual or as demonstrated by a Stryker representative; (4)
products on which any original serial numbers or other identification marks have been removed or destroyed; (5) products
that have been repaired with any unauthorized or non-Stryker components; or (6) failure to follow the instructions for use.
If a valid warranty claim is received within thirty (30) days of the expiration of the applicable warranty period, Stryker will, in
its sole discretion: (1) replace the product at no charge with a product that is at least functionally equivalent to the original
product or (2) refund the purchase price of the product. If a refund is provided by Stryker, the product for which the refund is
provided must be returned to Stryker and will become Stryker’s property. In any event, Stryker’s liability for breach of
warranty shall be limited to the replacement value of the defective or non-conforming part or component.
If Stryker determines in its reasonable discretion that the claimed defect or non-conformance in the product is excluded from
warranty coverage as described hereunder, it will notify the customer of such determination and will provide an estimate of
the cost of repair of the product. In such an event, any repair would be performed at Stryker’s standard rates.
Products and product components repaired or replaced under this warranty continue to be warranted as described herein
during the initial applicable warranty period or, if the initial warranty period has expired by the time the product is repaired
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or replaced, for thirty (30) days after delivery of the repaired or replaced product. When a product or component is replaced,
the item provided in replacement will be the customer’s property and the replaced item will be Stryker’s property. If a refund
is provided by Stryker, the product for which the refund is provided must be returned to Stryker and will become Stryker’s
property.
Sensormat®, STANLEY®, Bed-Check®, UMP®, and Micro-Tech® are registered trademarks of STANLEY® Security Solutions, Inc.
HAS EL10104 Rev. C 06/2020
The OEM information listed on the label is provided as device ID prior to reprocessing and may contain the trademarks of unrelated
third parties that do not sponsor this device.
This product and its packaging have been exposed to ethylene oxide gas (EtO). Even though the product then is processed in compliance
with all applicable laws and regulations relating to EtO exposure, Proposition 65, a State of California voter initiative, requires the
following notice:
Warning: This product and its packaging have been exposed to ethylene oxide. The packaging may expose you to ethylene oxide, a
chemical known to the State of California to cause cancer or birth defects or other reproductive harm.
Warning: This product can expose you to chemicals including Nickel, which is known to the State of California to cause cancer. For more
information go to www.P65Warnings.ca.gov.
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